Christopher P Barnett

5PUBLICATIONS
29CO-AUTHORS
Foetal development and medicineCardiology (incl. cardiovascular diseases)Gene and molecular therapyNeonatologyEpigenetics (incl. genome methylation and epigenomics)
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Publications (5)

|Apr 05, 2024
Extending the new era of genomic testing into pregnancy management: A proposed model for Australian prenatal services.

Alice Rogers, Lucas De Jong, Wendy Waters

|Mar 02, 2022
Pathogenic variants in MDFIC cause recessive central conducting lymphatic anomaly with lymphedema.

Alicia B Byrne, Pascal Brouillard, Drew L Sutton

|May 01, 2021
A de novo missense variant in MED13 in a patient with global developmental delay, marked facial dysmorphism, macroglossia, short stature, and macrocephaly.

Alice P Rogers, Kathryn Friend, Lesley Rawlings

|Apr 25, 2020
Novel de novo 2q14.3 deletion disrupting CNTNAP5 in a girl with intellectual impairment, thin corpus callosum, and microcephaly.

Eleanor G Ludington, Sui Yu, Ha Ae Bae

|Apr 18, 2020
CDH1-related blepharocheilodontic syndrome is associated with diffuse gastric cancer risk.

Shannon LeBlanc, Dildeepa Naveen, Eric Haan

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Frequent Collaborators

1 joint publications

Shannon LeBlanc

1 joint publications

Alicia B Byrne

1 joint publications

Pascal Brouillard

1 joint publications

Drew L Sutton